[1-(2-(4-Chloro-benzenesulfonylamino)-1-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-ethylsulfanylmethyl)-cyclopropyl]-acetic acid benzyl ester

Base Information

Chemical Name:[1-(2-(4-Chloro-benzenesulfonylamino)-1-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-ethylsulfanylmethyl)-cyclopropyl]-acetic acid benzyl ester
CAS No.:904916-32-1
Molecular Formula:C₃₈H₃₄Cl₂N₂O₄S₂
Molecular Weight:717.737
Hs Code.:

[1-(2-(4-Chloro-benzenesulfonylamino)-1-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-ethylsulfanylmethyl)-cyclopropyl]-acetic acid benzyl ester

Synonyms:[1-(2-(4-Chloro-benzenesulfonylamino)-1-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-ethylsulfanylmethyl)-cyclopropyl]-acetic acid benzyl ester

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Chemical Property of [1-(2-(4-Chloro-benzenesulfonylamino)-1-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-ethylsulfanylmethyl)-cyclopropyl]-acetic acid benzyl ester

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Technology Process of [1-(2-(4-Chloro-benzenesulfonylamino)-1-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-ethylsulfanylmethyl)-cyclopropyl]-acetic acid benzyl ester

There total 12 articles about [1-(2-(4-Chloro-benzenesulfonylamino)-1-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-ethylsulfanylmethyl)-cyclopropyl]-acetic acid benzyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: [1-(2-Amino-1-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-ethylsulfanylmethyl)-cyclopropyl]-acetic acid benzyl ester

: 98-60-2
4-chlorobenzenesulfonyl chloride

: 904916-32-1
[1-(2-(4-Chloro-benzenesulfonylamino)-1-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-ethylsulfanylmethyl)-cyclopropyl]-acetic acid benzyl ester

Guidance literature:: With triethylamine; In 1,2-dichloro-ethane; at 5 ℃; for 12h;
DOI:10.1248/cpb.54.603

Reference yield:

: benzyl (1-mercaptomethylcyclopropyl)acetate

: 904916-32-1
[1-(2-(4-Chloro-benzenesulfonylamino)-1-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-ethylsulfanylmethyl)-cyclopropyl]-acetic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 46 percent / cesium carbonate / dimethylsulfoxide / 1 h / 20 °C

2: methylhydrazine / ethanol; dioxane / 7 h / Heating

3: triethylamine / 1,2-dichloro-ethane / 12 h / 5 °C

With caesium carbonate; triethylamine; methylhydrazine; In 1,4-dioxane; ethanol; dimethyl sulfoxide; 1,2-dichloro-ethane;
DOI:10.1248/cpb.54.603

Reference yield:

: 203940-17-4
methyl 3-[(E)-2-(7-chloro-2-quinolyl)vinyl]benzoate

: 904916-32-1
[1-(2-(4-Chloro-benzenesulfonylamino)-1-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-ethylsulfanylmethyl)-cyclopropyl]-acetic acid benzyl ester

Guidance literature:: Multi-step reaction with 9 steps

1: aq. NaOH / tetrahydrofuran; methanol / 3 h / 40 °C

2: 93 percent / K₂CO₃*1.5H₂O; diphenylphosphoryl azide / dimethylformamide / 20 h / 20 °C

3: 98 percent / aq. HCl / ethanol / 6 h / Heating

4: 55 percent / sodium borohydride; potassium carbonate / ethanol / 1 h / 20 °C

5: 18.8 g / toluene / 3 h / 160 °C / 3 Torr

6: 19.0 g / pyridine / 1,2-dichloro-ethane / 12 h / 20 °C

7: 46 percent / cesium carbonate / dimethylsulfoxide / 1 h / 20 °C

8: methylhydrazine / ethanol; dioxane / 7 h / Heating

9: triethylamine / 1,2-dichloro-ethane / 12 h / 5 °C

With pyridine; hydrogenchloride; sodium hydroxide; sodium tetrahydroborate; diphenylphosphoranyl azide; potassium carbonate; caesium carbonate; triethylamine; methylhydrazine; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dimethyl sulfoxide; 1,2-dichloro-ethane; N,N-dimethyl-formamide; toluene;
DOI:10.1248/cpb.54.603